AU736608B2 - Epoxy resin mixtures - Google Patents
Epoxy resin mixtures Download PDFInfo
- Publication number
- AU736608B2 AU736608B2 AU46144/97A AU4614497A AU736608B2 AU 736608 B2 AU736608 B2 AU 736608B2 AU 46144/97 A AU46144/97 A AU 46144/97A AU 4614497 A AU4614497 A AU 4614497A AU 736608 B2 AU736608 B2 AU 736608B2
- Authority
- AU
- Australia
- Prior art keywords
- epoxy resin
- resin mixture
- component
- epoxide
- materials
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 69
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 68
- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 16
- 150000002118 epoxides Chemical group 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 12
- -1 phosphorus compound Chemical class 0.000 claims abstract description 12
- 238000002347 injection Methods 0.000 claims abstract description 11
- 239000007924 injection Substances 0.000 claims abstract description 11
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 11
- 239000011574 phosphorus Substances 0.000 claims abstract description 11
- 239000004848 polyfunctional curative Substances 0.000 claims abstract description 10
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 8
- 125000003118 aryl group Chemical group 0.000 claims abstract description 8
- 229920000768 polyamine Polymers 0.000 claims abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
- 230000008030 elimination Effects 0.000 claims abstract description 3
- 238000003379 elimination reaction Methods 0.000 claims abstract description 3
- 229920005989 resin Polymers 0.000 claims description 25
- 239000011347 resin Substances 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 18
- 239000002131 composite material Substances 0.000 claims description 15
- 239000012779 reinforcing material Substances 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 6
- 230000000052 comparative effect Effects 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000006261 foam material Substances 0.000 claims description 4
- 239000004745 nonwoven fabric Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 239000005350 fused silica glass Substances 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052717 sulfur Chemical group 0.000 claims description 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004035 construction material Substances 0.000 claims description 2
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 claims description 2
- 238000009413 insulation Methods 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- XNQULTQRGBXLIA-UHFFFAOYSA-O phosphonic anhydride Chemical compound O[P+](O)=O XNQULTQRGBXLIA-UHFFFAOYSA-O 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims 1
- 239000012774 insulation material Substances 0.000 claims 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical class N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 7
- 238000012360 testing method Methods 0.000 description 19
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 8
- 239000003063 flame retardant Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- 230000009477 glass transition Effects 0.000 description 7
- 238000010276 construction Methods 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 238000002485 combustion reaction Methods 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 150000003018 phosphorus compounds Chemical class 0.000 description 5
- 239000000779 smoke Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 238000011417 postcuring Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 238000009745 resin transfer moulding Methods 0.000 description 3
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 2
- PAQZWJGSJMLPMG-UHFFFAOYSA-N 2,4,6-tripropyl-1,3,5,2$l^{5},4$l^{5},6$l^{5}-trioxatriphosphinane 2,4,6-trioxide Chemical compound CCCP1(=O)OP(=O)(CCC)OP(=O)(CCC)O1 PAQZWJGSJMLPMG-UHFFFAOYSA-N 0.000 description 2
- HPILSDOMLLYBQF-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COC(CCC)OCC1CO1 HPILSDOMLLYBQF-UHFFFAOYSA-N 0.000 description 2
- BZVQIZYWIWXTHX-UHFFFAOYSA-N 2-[[methyl(oxiran-2-ylmethoxy)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(C)OCC1CO1 BZVQIZYWIWXTHX-UHFFFAOYSA-N 0.000 description 2
- KQCDNTFMEXGZKZ-UHFFFAOYSA-N 2-[[oxiran-2-ylmethoxy(phenyl)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(C=1C=CC=CC=1)(=O)OCC1CO1 KQCDNTFMEXGZKZ-UHFFFAOYSA-N 0.000 description 2
- BBMRRJMOHHHXJB-UHFFFAOYSA-N 2-[[oxiran-2-ylmethoxy(propyl)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(CCC)OCC1CO1 BBMRRJMOHHHXJB-UHFFFAOYSA-N 0.000 description 2
- ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 150000003009 phosphonic acids Chemical class 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 230000000930 thermomechanical effect Effects 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- GRLNGTRKIXFDEG-UHFFFAOYSA-N (4-methoxyphenyl) bis(oxiran-2-ylmethyl) phosphate Chemical compound C1=CC(OC)=CC=C1OP(=O)(OCC1OC1)OCC1OC1 GRLNGTRKIXFDEG-UHFFFAOYSA-N 0.000 description 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- VBWUAHLEBGOEQM-UHFFFAOYSA-N 2-(diethylphosphoryloxymethyl)oxirane Chemical compound CCP(=O)(CC)OCC1CO1 VBWUAHLEBGOEQM-UHFFFAOYSA-N 0.000 description 1
- XRAKMBFIMURQJO-UHFFFAOYSA-N 2-(dimethylphosphoryloxymethyl)oxirane Chemical compound CP(C)(=O)OCC1CO1 XRAKMBFIMURQJO-UHFFFAOYSA-N 0.000 description 1
- HSDVRWZKEDRBAG-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COC(CCCCC)OCC1CO1 HSDVRWZKEDRBAG-UHFFFAOYSA-N 0.000 description 1
- ZXUZCXVFPLSUAU-UHFFFAOYSA-N 2-[[4-[1,1,2-tris[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=1C=CC(OCC2OC2)=CC=1)(C=1C=CC(OCC2OC2)=CC=1)C(C=C1)=CC=C1OCC1CO1 ZXUZCXVFPLSUAU-UHFFFAOYSA-N 0.000 description 1
- CUEKQHFEMQNDMT-UHFFFAOYSA-N 2-[[4-[1,1,2-tris[4-(oxiran-2-ylmethyl)phenyl]ethyl]phenyl]methyl]oxirane Chemical compound C=1C=C(CC(C=2C=CC(CC3OC3)=CC=2)(C=2C=CC(CC3OC3)=CC=2)C=2C=CC(CC3OC3)=CC=2)C=CC=1CC1CO1 CUEKQHFEMQNDMT-UHFFFAOYSA-N 0.000 description 1
- ITMUVRJKHDNAJM-UHFFFAOYSA-N 2-[[butyl(oxiran-2-ylmethoxy)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(CCCC)OCC1CO1 ITMUVRJKHDNAJM-UHFFFAOYSA-N 0.000 description 1
- WCEQJLAETAQVIG-UHFFFAOYSA-N 2-[[ethenyl(oxiran-2-ylmethoxy)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(C=C)OCC1CO1 WCEQJLAETAQVIG-UHFFFAOYSA-N 0.000 description 1
- OIYQFLTVNXTWJA-UHFFFAOYSA-N 2-[[ethyl(methyl)phosphoryl]oxymethyl]oxirane Chemical compound CCP(C)(=O)OCC1CO1 OIYQFLTVNXTWJA-UHFFFAOYSA-N 0.000 description 1
- JQXLMHHSBCDJAV-UHFFFAOYSA-N 2-[[ethyl(oxiran-2-ylmethoxy)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(CC)OCC1CO1 JQXLMHHSBCDJAV-UHFFFAOYSA-N 0.000 description 1
- RJPFDYYLINHULQ-UHFFFAOYSA-N 2-[[oxiran-2-ylmethoxy-(2-phenylphenyl)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(C=1C(=CC=CC=1)C=1C=CC=CC=1)(=O)OCC1CO1 RJPFDYYLINHULQ-UHFFFAOYSA-N 0.000 description 1
- ZEWITWPJAPXMBF-UHFFFAOYSA-N 2-methylpropyl bis(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(=O)(OCC(C)C)OCC1CO1 ZEWITWPJAPXMBF-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- AHIPJALLQVEEQF-UHFFFAOYSA-N 4-(oxiran-2-ylmethoxy)-n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1COC(C=C1)=CC=C1N(CC1OC1)CC1CO1 AHIPJALLQVEEQF-UHFFFAOYSA-N 0.000 description 1
- FAUAZXVRLVIARB-UHFFFAOYSA-N 4-[[4-[bis(oxiran-2-ylmethyl)amino]phenyl]methyl]-n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC(CC=2C=CC(=CC=2)N(CC2OC2)CC2OC2)=CC=1)CC1CO1 FAUAZXVRLVIARB-UHFFFAOYSA-N 0.000 description 1
- CXXSQMDHHYTRKY-UHFFFAOYSA-N 4-amino-2,3,5-tris(oxiran-2-ylmethyl)phenol Chemical compound C1=C(O)C(CC2OC2)=C(CC2OC2)C(N)=C1CC1CO1 CXXSQMDHHYTRKY-UHFFFAOYSA-N 0.000 description 1
- 102100030154 CDC42 small effector protein 1 Human genes 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- NJLHHACGWKAWKL-UHFFFAOYSA-N ClP(Cl)=O Chemical class ClP(Cl)=O NJLHHACGWKAWKL-UHFFFAOYSA-N 0.000 description 1
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 101000794295 Homo sapiens CDC42 small effector protein 1 Proteins 0.000 description 1
- 208000022976 Liberfarb syndrome Diseases 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- VQIORMMVMPUJKE-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) (4-propan-2-yloxyphenyl) phosphate Chemical compound C1=CC(OC(C)C)=CC=C1OP(=O)(OCC1OC1)OCC1OC1 VQIORMMVMPUJKE-UHFFFAOYSA-N 0.000 description 1
- JPUXKPLKGNXKKY-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) (4-propoxyphenyl) phosphate Chemical compound C1=CC(OCCC)=CC=C1OP(=O)(OCC1OC1)OCC1OC1 JPUXKPLKGNXKKY-UHFFFAOYSA-N 0.000 description 1
- IQGRJDMCADTKHH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) hydrogen phosphate Chemical compound C1OC1COP(=O)(O)OCC1CO1 IQGRJDMCADTKHH-UHFFFAOYSA-N 0.000 description 1
- HLVMEDJYWHPKKB-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) phenyl phosphate Chemical compound C1OC1COP(OC=1C=CC=CC=1)(=O)OCC1CO1 HLVMEDJYWHPKKB-UHFFFAOYSA-N 0.000 description 1
- UPTYJLVSOWTXOS-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) phenylsulfanyl phosphate Chemical compound C1OC1COP(OSC=1C=CC=CC=1)(=O)OCC1CO1 UPTYJLVSOWTXOS-UHFFFAOYSA-N 0.000 description 1
- DFYQRFUGSMMBTG-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) propyl phosphate Chemical compound C1OC1COP(=O)(OCCC)OCC1CO1 DFYQRFUGSMMBTG-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- VMUSTDHWEXDYOI-UHFFFAOYSA-N butyl bis(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(=O)(OCCCC)OCC1CO1 VMUSTDHWEXDYOI-UHFFFAOYSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 150000007973 cyanuric acids Chemical class 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- PPQREHKVAOVYBT-UHFFFAOYSA-H dialuminum;tricarbonate Chemical class [Al+3].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O PPQREHKVAOVYBT-UHFFFAOYSA-H 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- DHPWUANXTPYNBW-UHFFFAOYSA-N ethyl bis(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(=O)(OCC)OCC1CO1 DHPWUANXTPYNBW-UHFFFAOYSA-N 0.000 description 1
- GWOZYVBICFETJW-UHFFFAOYSA-N ethyl oxiran-2-ylmethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC1CO1 GWOZYVBICFETJW-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000007496 glass forming Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- UPDJEKZEIXEFOD-UHFFFAOYSA-N hydroxy-bis(oxiran-2-ylmethoxy)-sulfanylidene-lambda5-phosphane Chemical compound C1OC1COP(=S)(O)OCC1CO1 UPDJEKZEIXEFOD-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical class [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 235000012254 magnesium hydroxide Nutrition 0.000 description 1
- KQEBVGPNOBFTJP-UHFFFAOYSA-N methyl bis(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(=O)(OC)OCC1CO1 KQEBVGPNOBFTJP-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- IGALFTFNPPBUDN-UHFFFAOYSA-N phenyl-[2,3,4,5-tetrakis(oxiran-2-ylmethyl)phenyl]methanediamine Chemical compound C=1C(CC2OC2)=C(CC2OC2)C(CC2OC2)=C(CC2OC2)C=1C(N)(N)C1=CC=CC=C1 IGALFTFNPPBUDN-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical class ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- ZNZJJSYHZBXQSM-UHFFFAOYSA-N propane-2,2-diamine Chemical compound CC(C)(N)N ZNZJJSYHZBXQSM-UHFFFAOYSA-N 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- PYGKDFLMCGZPHX-UHFFFAOYSA-N tris(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(OCC1OC1)(=O)OCC1CO1 PYGKDFLMCGZPHX-UHFFFAOYSA-N 0.000 description 1
- MVPHRFAZBSCNLO-UHFFFAOYSA-N tris[3-(oxiran-2-yl)propyl] phosphate Chemical compound C1OC1CCCOP(OCCCC1OC1)(=O)OCCCC1CO1 MVPHRFAZBSCNLO-UHFFFAOYSA-N 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/30—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
- C08G59/304—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3254—Epoxy compounds containing three or more epoxy groups containing atoms other than carbon, hydrogen, oxygen or nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/24994—Fiber embedded in or on the surface of a polymeric matrix
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19639720 | 1996-09-26 | ||
| DE19639720 | 1996-09-26 | ||
| PCT/DE1997/002019 WO1998013407A1 (de) | 1996-09-26 | 1997-09-10 | Epoxidharzmischungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU4614497A AU4614497A (en) | 1998-04-17 |
| AU736608B2 true AU736608B2 (en) | 2001-08-02 |
Family
ID=7807060
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU46144/97A Ceased AU736608B2 (en) | 1996-09-26 | 1997-09-10 | Epoxy resin mixtures |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6201074B1 (cs) |
| EP (1) | EP0928304B1 (cs) |
| JP (1) | JP2001503790A (cs) |
| KR (1) | KR20000048654A (cs) |
| CN (1) | CN1233262A (cs) |
| AT (1) | ATE271574T1 (cs) |
| AU (1) | AU736608B2 (cs) |
| CA (1) | CA2266903A1 (cs) |
| CZ (1) | CZ98199A3 (cs) |
| DE (1) | DE59711794D1 (cs) |
| ES (1) | ES2224274T3 (cs) |
| PL (1) | PL332369A1 (cs) |
| SK (1) | SK32699A3 (cs) |
| WO (1) | WO1998013407A1 (cs) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19747553A1 (de) * | 1997-10-28 | 1999-04-29 | Siemens Ag | Epoxidharzmischung, daraus hergestellte Verbundwerkstoffe und deren Verwendung |
| DE19917428A1 (de) * | 1999-04-19 | 2000-10-26 | Clariant Gmbh | Flammwidrige phosphormodifizierte Epoxidharze |
| JP4798855B2 (ja) * | 2001-02-21 | 2011-10-19 | 株式会社Ａｄｅｋａ | 難燃性エポキシ樹脂組成物 |
| AT412089B8 (de) * | 2002-10-21 | 2004-10-25 | Surface Specialties Austria | Addukte von epoxidharzen und von phosphor abgeleiteten säuren sowie verfahren zu deren herstellung |
| JP5250972B2 (ja) | 2004-02-27 | 2013-07-31 | 東レ株式会社 | 炭素繊維強化複合材料用エポキシ樹脂組成物、プリプレグ、一体化成形品、繊維強化複合材料板、および電気・電子機器用筐体 |
| CN100591713C (zh) * | 2004-02-27 | 2010-02-24 | 东丽株式会社 | 碳纤维增强复合材料用环氧树脂组合物、预浸料坯、一体化成型品、纤维增强复合材料板及电气·电子设备用外壳 |
| KR101437699B1 (ko) * | 2006-04-24 | 2014-09-03 | 도레이 카부시키가이샤 | 에폭시 수지 조성물, 섬유 강화 복합 재료 및 그의 제조 방법 |
| US8815973B2 (en) | 2007-08-28 | 2014-08-26 | Pioneer Surgical Technology, Inc. | Cement products and methods of making and using the same |
| DE102009028019A1 (de) | 2009-02-04 | 2010-08-05 | Evonik Degussa Gmbh | Härtbare Zusammensetzungen auf Basis von Epoxidharzen und hetero-poly-cyclischen Polyaminen |
| US9139706B2 (en) * | 2010-03-30 | 2015-09-22 | Toray Industries, Inc. | Prepreg, fiber-reinforced composite material, and method for producing prepreg |
| CN103403054B (zh) * | 2011-03-22 | 2016-03-09 | 三菱丽阳株式会社 | 环氧树脂组合物、预浸料、纤维增强复合材料、电子电气设备用壳体 |
| CN103619994B (zh) | 2011-06-09 | 2016-09-07 | 巴斯夫欧洲公司 | 具有阻燃膦酸酯的硬化环氧树脂的制备 |
| JP5934580B2 (ja) * | 2011-06-13 | 2016-06-15 | 日東電工株式会社 | エポキシ樹脂多孔質膜、非水電解質蓄電デバイス用セパレータ、非水電解質蓄電デバイス、複合半透膜及びそれらの製造方法 |
| WO2014206487A1 (en) * | 2013-06-28 | 2014-12-31 | Fundacion Imdea Materiales | A halogen free flame retardant epoxy resin composition |
| JP2015040289A (ja) * | 2013-08-23 | 2015-03-02 | 三菱化学株式会社 | エポキシ樹脂、エポキシ樹脂組成物、硬化物及び電気・電子回路用積層板 |
| CN105111687B (zh) * | 2015-09-01 | 2017-07-18 | 沈阳化工大学 | 一种无卤环氧树脂阻燃剂及其制备方法 |
| DE102017204982A1 (de) * | 2017-03-24 | 2018-09-27 | Siemens Aktiengesellschaft | Faserverbundbauteil |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0384939A1 (de) * | 1989-03-03 | 1990-09-05 | Siemens Aktiengesellschaft | Epoxidharz-Formmassen |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2856369A (en) | 1953-05-08 | 1958-10-14 | Shell Dev | Epoxy-substituted esters of phosphoruscontaining acid and their polymers |
| US2766139A (en) | 1955-04-13 | 1956-10-09 | Masonite Corp | Method of producing fire resistant lignocellulose hardboard products |
| US3398019A (en) | 1963-02-21 | 1968-08-20 | Monsanto Co | Method for fireproofing cellulosic material |
| JPS51143620A (en) | 1975-06-06 | 1976-12-10 | Matsumoto Seiyaku Kogyo Kk | Process for preparation of epoxydiphosphonate |
| DE2538675A1 (de) * | 1975-08-30 | 1977-03-03 | Hoechst Ag | Verfahren zur herstellung von phosphorhaltigen epoxidharzen und ihre verwendung zur flammfestausruestung |
| GB8610067D0 (en) | 1986-04-24 | 1986-05-29 | Steetley Refractories Ltd | Coated magnesium hydroxide |
| ATE107677T1 (de) | 1989-03-03 | 1994-07-15 | Siemens Ag | Epoxidharzmischungen. |
| DE4237132C1 (de) | 1992-11-03 | 1994-07-07 | Siemens Ag | UV-aktiviert thermisch härtendes einkomponentiges Reaktionsharzsystem |
| DE4308187A1 (de) | 1993-03-15 | 1994-09-22 | Siemens Ag | Epoxidharzmischungen |
| DE4340834A1 (de) * | 1993-03-15 | 1994-09-22 | Siemens Ag | Phosphormodifizierte Epoxidharze, Verfahren zu ihrer Herstellung sowie ihre Verwendung |
| JPH08507812A (ja) * | 1993-03-15 | 1996-08-20 | シーメンス・アクチェンゲゼルシャフト | リン変性エポキシ樹脂、その製造方法およびその用途 |
| DE4431751C1 (de) | 1994-09-06 | 1996-05-09 | Siemens Ag | Flammwidriges einkomponentiges Reaktionsharz |
| TW297034B (cs) | 1994-09-09 | 1997-02-01 | Siemens Ag | |
| TW294694B (cs) | 1994-09-09 | 1997-01-01 | Siemens Ag | |
| TW294693B (cs) | 1994-09-09 | 1997-01-01 | Siemens Ag | |
| DE19506010A1 (de) | 1995-02-17 | 1996-08-22 | Siemens Ag | Flammwidriges Reaktionsharzsystem |
| JPH11500150A (ja) | 1995-01-26 | 1999-01-06 | シーメンス アクチエンゲゼルシヤフト | 燐含有成分を有する反応性樹脂系 |
-
1997
- 1997-09-10 CZ CZ99981A patent/CZ98199A3/cs unknown
- 1997-09-10 SK SK326-99A patent/SK32699A3/sk unknown
- 1997-09-10 EP EP19970944695 patent/EP0928304B1/de not_active Expired - Lifetime
- 1997-09-10 WO PCT/DE1997/002019 patent/WO1998013407A1/de not_active Application Discontinuation
- 1997-09-10 DE DE59711794T patent/DE59711794D1/de not_active Expired - Lifetime
- 1997-09-10 JP JP51513498A patent/JP2001503790A/ja active Pending
- 1997-09-10 ES ES97944695T patent/ES2224274T3/es not_active Expired - Lifetime
- 1997-09-10 PL PL33236997A patent/PL332369A1/xx unknown
- 1997-09-10 KR KR1019990702598A patent/KR20000048654A/ko not_active Ceased
- 1997-09-10 US US09/269,543 patent/US6201074B1/en not_active Expired - Fee Related
- 1997-09-10 AU AU46144/97A patent/AU736608B2/en not_active Ceased
- 1997-09-10 CN CN97198799A patent/CN1233262A/zh active Pending
- 1997-09-10 AT AT97944695T patent/ATE271574T1/de active
- 1997-09-10 CA CA 2266903 patent/CA2266903A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0384939A1 (de) * | 1989-03-03 | 1990-09-05 | Siemens Aktiengesellschaft | Epoxidharz-Formmassen |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE271574T1 (de) | 2004-08-15 |
| CA2266903A1 (en) | 1998-04-02 |
| AU4614497A (en) | 1998-04-17 |
| CZ98199A3 (cs) | 1999-08-11 |
| PL332369A1 (en) | 1999-09-13 |
| EP0928304A1 (de) | 1999-07-14 |
| US6201074B1 (en) | 2001-03-13 |
| WO1998013407A1 (de) | 1998-04-02 |
| JP2001503790A (ja) | 2001-03-21 |
| EP0928304B1 (de) | 2004-07-21 |
| KR20000048654A (ko) | 2000-07-25 |
| SK32699A3 (en) | 2000-06-12 |
| CN1233262A (zh) | 1999-10-27 |
| ES2224274T3 (es) | 2005-03-01 |
| DE59711794D1 (de) | 2004-08-26 |
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